An integrated knowledge database dedicated to ncRNAs, especially lncRNAs.
Detail infomation of NONHSAG012905.2

General info


NONCODE GENE IDNONHSAG012905.2
Chromosomechr13
Start Site19736976
End Site19737254
Strand-
Length278
Assemblyhg38
ClassLinc;
Other Gene VersionsNONHSAG012905.1(old version)

Transcripts in Gene


NONCODE TRANSCRIPT ID
NONHSAT032288.2

Expression Profile (Data Source:Human Body Map)


adiposeadrenalbrainbrain_Rbreastcolon
000000
foreskinheartheart_RHLF_1HLF_2kidney
000000
liverliver_RlunglymphNodeovaryplacenta_R
000000
prostateskeltalMuscletestestestes_RthyroidwhiteBloodCell
000.405952000
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Exosome Expression Profile (Data Source: NCBI GEO)


A431_cellLine
(Squamous Cell Carcinoma Cell Line Exosomes)
BJ_cellLine
(Foreskin Fibroblast Cell Line Exosomes)
HepG2_cellLine
(Hepatocellular Carcinoma Cell Line Exosomes)
HUVEC_cellLine
(Human Umbilical Vein Endothelial Cell Line Exosomes)
invasive_NFPAs
(Invasive Non-functional Pituitary Adenomas Exosomes)
013.4021013.968913.0833
non-invasive_NFPAs
(Non-invasive Non-functional Pituitary Adenomas Exosomes)
MCF7_cellLine
(Human Breast Cancer Cell Line Exosomes)
MDA-MB-231_cellLine
(Human Breast Cancer Cell Line Exosomes)
tuberculosis_patients_serum
(Active Tuberculosis Patients Serum Exosomes)
normal_people_blood
(Normal People Blood Exosomes)
5.547380013.37715.83089
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Expression Profile (Data Source: Single Cell)


Conservation Info


Note: T = There are transcripts in this region.


Disease related


Disease:

NONCODE IDGene SymbolDisease nameSource DatabaseSource PMID
NONHSAG012905.27SLAIDS,dermatomyositisLncRNAWiki0
NONHSAG012905.27SLAIDSLncRNADisease20926562
NONHSAG012905.27SLAIDSLncRNADisease16489186
NONHSAG012905.27SLdermatomyositisLncRNADisease16142868
NONHSAG012905.27SLLeishmaniaLncRNADisease15955815
NONHSAG012905.27SLLeishmaniaLncRNADisease20392923
NONHSAG012905.27SLLeishmaniaLncRNADisease20856851
NONHSAG012905.27SLLeishmaniaLncRNADisease20561310
NONHSAG012905.27SLpolymyositisLncRNADisease16142868

Mutations:

NONCODE IDSNP IDGWAS traitSource PMID